Sr. R&D Engineer (Product Development Activities)

Description

Demonstrated experience writing complex Design Verification plans, protocols, reports
Proficiency with statistical techniques including Minitab to analyze data, generate appropriate plots/graphs required to show performance against acceptance criteria for DV reports
Ability to write and get cross-functional support for engineering rationales used to support product development activities
Demonstrated ability to execute Design Verification testing, including building samples, adherence to test protocols/test methods, responsible data collection/preparation practices, and good lab practices.
Demonstrated ability to clearly and effectively communicate (verbal & written) concepts and ideas to technical and non-technical team members in a way that articulates problem statement, investigating approach, possible solutions, final recommendation, and implementation plan
Strong decision-making capability, even with limited or ambiguous information with the ability to absorb information and solve complex problems quickly
Demonstrated industry or academic experience driving product development in a cross-functional team setting to solve complex problems and meet milestones

Requirements

Minimum 6 years of experience as a product design / development engineer in the medical device, pharmaceutical or other regulated industry (experience with FDA class II or III medical devices preferred). Bachelor’s degree required in Mechanical or Biomedical Engineering (Mechanics focus). Master Degree or above preferred.

Pay

TBD

Schedule

1st Shift